32,225 research outputs found
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Microbial metal resistance and metabolism across dynamic landscapes: high-throughput environmental microbiology.
Multidimensional gradients of inorganic compounds influence microbial activity in diverse pristine and anthropogenically perturbed environments. Here, we suggest that high-throughput cultivation and genetics can be systematically applied to generate quantitative models linking gene function, microbial community activity, and geochemical parameters. Metal resistance determinants represent a uniquely universal set of parameters around which to study and evaluate microbial fitness because they represent a record of the environment in which all microbial life evolved. By cultivating microbial isolates and enrichments in laboratory gradients of inorganic ions, we can generate quantitative predictions of limits on microbial range in the environment, obtain more accurate gene annotations, and identify useful strategies for predicting and engineering the trajectory of natural ecosystems
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Large-effect flowering time mutations reveal conditionally adaptive paths through fitness landscapes in Arabidopsis thaliana.
Contrary to previous assumptions that most mutations are deleterious, there is increasing evidence for persistence of large-effect mutations in natural populations. A possible explanation for these observations is that mutant phenotypes and fitness may depend upon the specific environmental conditions to which a mutant is exposed. Here, we tested this hypothesis by growing large-effect flowering time mutants of Arabidopsis thaliana in multiple field sites and seasons to quantify their fitness effects in realistic natural conditions. By constructing environment-specific fitness landscapes based on flowering time and branching architecture, we observed that a subset of mutations increased fitness, but only in specific environments. These mutations increased fitness via different paths: through shifting flowering time, branching, or both. Branching was under stronger selection, but flowering time was more genetically variable, pointing to the importance of indirect selection on mutations through their pleiotropic effects on multiple phenotypes. Finally, mutations in hub genes with greater connectedness in their regulatory networks had greater effects on both phenotypes and fitness. Together, these findings indicate that large-effect mutations may persist in populations because they influence traits that are adaptive only under specific environmental conditions. Understanding their evolutionary dynamics therefore requires measuring their effects in multiple natural environments
The Benefits of Local Forest Recreation in Austria and Its Dependence on Naturalness and Quietude
The benefits of local recreation in the State-owned forests in Austria (i.e., about 15% of all Austrian forests) are ascertained in this paper. A representative survey of households dealt with their local recreation, perceptions of and disturbances in forests. Total annual benefits of local recreation activities in State-owned forests, such as walking, hiking, cycling and wildlife observation, amount to about EUR 500 per person. Based on the respondents’ valuation of the degree of naturalness and quietude, as well as the options of forest management, the current management increases recreation benefits by EUR 13 per person through increased naturalness, and EUR 1.30 per person and year through increased quietude. Emphasis was placed on the benefits of the current management regime of multifunctional forestry compared to the benefits of a baseline scenario that was drafted specifically for this study, assuming higher levels of lumbering up to the limits allowed by existing nature conservation and forestry laws. The results suggest that forest management has a higher impact on recreational benefits through the naturalness of forests than through reducing artificial noise. A more sustainable forest management could further increase the benefits people derive from both naturalness and lower levels of artificial noise
Strong Selection Significantly Increases Epistatic Interactions in the Long-Term Evolution of a Protein
Epistatic interactions between residues determine a protein's adaptability
and shape its evolutionary trajectory. When a protein experiences a changed
environment, it is under strong selection to find a peak in the new fitness
landscape. It has been shown that strong selection increases epistatic
interactions as well as the ruggedness of the fitness landscape, but little is
known about how the epistatic interactions change under selection in the
long-term evolution of a protein. Here we analyze the evolution of epistasis in
the protease of the human immunodeficiency virus type 1 (HIV-1) using protease
sequences collected for almost a decade from both treated and untreated
patients, to understand how epistasis changes and how those changes impact the
long-term evolvability of a protein. We use an information-theoretic proxy for
epistasis that quantifies the co-variation between sites, and show that
positive information is a necessary (but not sufficient) condition that detects
epistasis in most cases. We analyze the "fossils" of the evolutionary
trajectories of the protein contained in the sequence data, and show that
epistasis continues to enrich under strong selection, but not for proteins
whose environment is unchanged. The increase in epistasis compensates for the
information loss due to sequence variability brought about by treatment, and
facilitates adaptation in the increasingly rugged fitness landscape of
treatment. While epistasis is thought to enhance evolvability via
valley-crossing early-on in adaptation, it can hinder adaptation later when the
landscape has turned rugged. However, we find no evidence that the HIV-1
protease has reached its potential for evolution after 9 years of adapting to a
drug environment that itself is constantly changing.Comment: 25 pages, 9 figures, plus Supplementary Material including
Supplementary Text S1-S7, Supplementary Tables S1-S2, and Supplementary
Figures S1-2. Version that appears in PLoS Genetic
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